acetylcarnitine and Ornithine Carbamoyltransferase Deficiency Disease

acetylcarnitine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 4 studies

Acetylcarnitine: An acetic acid ester of CARNITINE that facilitates movement of ACETYL COA into the matrices of mammalian MITOCHONDRIA during the oxidation of FATTY ACIDS.

Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)

Research

Studies (4)

Authors

Other Studies

4 other studies available for acetylcarnitine and Ornithine Carbamoyltransferase Deficiency Disease